EP0597115A1 - Parting agent - Google Patents
Parting agent Download PDFInfo
- Publication number
- EP0597115A1 EP0597115A1 EP93909426A EP93909426A EP0597115A1 EP 0597115 A1 EP0597115 A1 EP 0597115A1 EP 93909426 A EP93909426 A EP 93909426A EP 93909426 A EP93909426 A EP 93909426A EP 0597115 A1 EP0597115 A1 EP 0597115A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mold release
- release agent
- water
- good
- halogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 20
- 229920000570 polyether Polymers 0.000 claims abstract description 20
- 125000000524 functional group Chemical group 0.000 claims abstract description 11
- 239000006082 mold release agent Substances 0.000 claims description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 150000002367 halogens Chemical class 0.000 claims description 19
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- -1 phosphate ester Chemical class 0.000 claims description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000010702 perfluoropolyether Substances 0.000 claims description 3
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 238000003912 environmental pollution Methods 0.000 abstract description 4
- 238000000465 moulding Methods 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 241000047703 Nonion Species 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- 229920005830 Polyurethane Foam Polymers 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000012973 diazabicyclooctane Substances 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
- B29C33/60—Releasing, lubricating or separating agents
- B29C33/62—Releasing, lubricating or separating agents based on polymers or oligomers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2071/00—Use of polyethers, e.g. PEEK, i.e. polyether-etherketone or PEK, i.e. polyetherketone or derivatives thereof, as moulding material
Definitions
- the present invention relates to a mold release agent. Particularly, it relates to a water-based mold release agent used for the preparation of a shaped article of a polymeric material such as a synthetic resin and a rubber.
- an organic solvent-based mold release agent comprising a halogen-containing polyether as a main component
- a mold release agent comprising the halogen-containing polyether
- the water - based mold release agent comprising the halogen-containing polyether as the main component which is disclosed in Japanese Patent Kokai Publication No. 112610/1986 has the problem that the mold release agent has poor storage stability (namely, the halogen-containing polyether is separated from the mold release agent).
- An object of the present invention is to provide a water - based mold release agent which is free from the environmental pollution problem during its use, which has excellent dispersibility, storage stability and mold releasability and which gives a good surface state to a molded article of a polymeric material.
- the present invention provides a water-based mold release agent comprising, as a main component, a halogen-containing polyether having at least one functional group.
- the mold release agent according to the present invention comprises
- the halogen-containing polyether used in the present invention has at least one functional group, and the halogen-containing polyether having no functional group which is described in Japanese Patent Kokai Publication No. 112610/1906 is not preferable in the present invention.
- the halogen-containing polyether having at least one functional group may be well-known one and is described in Japanese Patent Kokai Publication No. 131132/1989 (corresponding to US Patent No. 4,836,944, the disclosure of which is incorporated herein by reference), Japanese Patent Kokai Publication No. 134189/1991, Japanese Patent Kokai Publication No. 268664/1989 (corresponding to US Patent No. 5,004,544, the disclosure of which is incorporated herein by reference), and Japanese Patent Kokai Publication No. 132917/1991.
- a perfluoropolyether having at lease one functional group is preferable.
- Specific examples of the preferable halogen-containing polyether are wherein R is m is 1 to 50, n is 1 to 100, p is 0 to 100, q is 0 to 100 and r is 1 to 50.
- a perfluoropolyether having a carboxylic acid group or salt thereof is preferable in view of the adherence to a mold surface.
- the halogen-containing polyether preferably has an average molecular weight of 1,000 to 5,000, more preferably 1,500 to 3,500.
- the surfactant used in the present invention may be any of a hydrocarbon surfactant and a fluorine-containing surfactant.
- Specific examples of the surfactant are Rapizol B-80 (manufactured by Nippon Oil and Fats Co., Ltd.), Nonion NS 230 (manufactured by Nippon Oil and Fats Co., Ltd.), Nonion NS 220 (manufactured by Nippon Oil and Fats Co., Ltd.), Unidine DS 403 (Daikin Industries Ltd.).
- the nonionic surfactant is preferable in view of the storage stability.
- the mold release agent is transparent (no cloudiness) and has remarkably excellent storage stability.
- the water-based mold release agent according to the present invention can be prepared, for example, by emulsifying the halogen-containing polyether, the surfactant and water by an ultrasonic homogenizer.
- the water-based mold release agent according to the present invention may further contains d) a phosphate ester or a salt thereof having a pefluoroalkyl group having 4 to 20 carbon atoms.
- a phosphate ester or a salt thereof having a pefluoroalkyl group having 4 to 20 carbon atoms Specific examples of the perfluoroalkyl group-containing phosphate ester are wherein m is 1 to 9, n is 1, 2 or 3.
- the halogen - containing polyether is emulsified in water and then the perfluoroalkyl group-containing phosphate ester is added to the emulsion.
- the phosphate ester having the perfluoroalkyl group having 4 to 20 carbon atoms gives, for example, excellent releasability for a urethane.
- the water-based mold release agent according to the present invention may contain a silicone or wax compound.
- the silicone or wax compound improves the surface state of the shaped article so as to reduce a cell collapse, particularly in the case of the polyurethane foam which tends to have the cell collapse.
- silicone compound examples are a silicone oil, a silicone resin, a mixture of silicone oil and resin.
- wax compound is a paraffinic wax.
- the water-based mold release agent according to the present invention comprises
- the amount of silicone or wax compound is from 0 to 5.0 parts by weight, preferably from 0 to 1.0 parts by weight per 1 part by weight of the halogen-containing polyether.
- the water-based mold release agent according to the present invention may contain usually 0.1 to 20 % by weight, preferably 0.5 to 10 % by weight of the components other than water c).
- the mold release agent can be used in a low concentration, migrates to the shaped article in a very low amount, and gives an easy post-treatment (good coating property and adhesion property).
- the mold release agent according to the present invention can be used as an internal mold release agent, but it is preferably used as an external mold release agent.
- any of a brush coating method, a dip coating method, a spray coating method and the like can be used.
- the mold release agent according to the present invention is useful for the preparation of the shaped article made of a synthetic resin and a rubber, particularly a polyurethane or a polyurea.
- a mold release agent was prepared by emulsifying the components shown in Table 1 at 25°C for 6 minutes by the use of an ultrasonic homogenizer (manufactured by Choonpakogyo Co. Ltd., Output: 300 W).
- the mold release agent was coated on a mold, and a urethane foam was molded from a liquid A and a liquid B shown in Table 2.
- the mold releasability and the surface state of the shaped article were evaluated.
- a mold release stress (g/cm2) was measured by the use of an autographic device (manufactured by Shimadzu Corp., DCM-50M). The results are shown in Table 3.
- Table 3 also show stability of the mold release agent.
- Table 2 Liquid A Sannix FA-912 Polyol 100 pbw manufactured by Sanyo Chemical Industries Ltd.
- Stability Mold releasability (g/cm2) Surface state 1 Good 160 Good 2 Good 170 Good 3 Good 95 Good 4 Very good 110 Good 5 Very good 125 Good 6 Very good 150 Good 7 Good 150 Good 8 Good 230 Good 9 Good 100 Good 10 Good 150 Good 11 Good 160 Good Com. 1 Bad 190 Good Com. 2 Very good 230 Pinholes formed Com. 3 Very good 300 Good Com. 4 Very good 350 Good Note) Stability: Very Good: Transparent (not separated after two weeks) Good: Milky white (separated after one week) Bad: Milky white (separated after two days) Surface state: Good: No cell collapse
- the water-based mold release agent according to the present invention gives no environmental pollution, has excellent dispersibility, storage stability and mold releasability and gives a good surface state to the shaped article of the polymeric material.
- the water-based mold release agent according to the present invention forms a reversed micelle having the functional group present in water.
- the water-based mold release agent according to the present invention is adsorbed easily and selectively by the mold surface and can form a tough coating film having good durability.
- the water-based mold release agent according to the present invention can give more uniform thickness of a coating film than an organic solvent - based mold release agent.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
Abstract
Description
- The present invention relates to a mold release agent. Particularly, it relates to a water-based mold release agent used for the preparation of a shaped article of a polymeric material such as a synthetic resin and a rubber.
- Hitherto, an organic solvent-based mold release agent comprising a halogen-containing polyether as a main component is known (cf. Japanese Patent Kokai Publication No. 112610/1986). Although the mold release agent comprising the halogen-containing polyether has good mold releasability, it has the problem that the environment is polluted during the use of it since it contains the organic solvent. It is required to develop a water-based mold release agent comprising a halogen-containing polyether as the main component; which is free from the environmental pollution. The water - based mold release agent comprising the halogen-containing polyether as the main component which is disclosed in Japanese Patent Kokai Publication No. 112610/1986 has the problem that the mold release agent has poor storage stability (namely, the halogen-containing polyether is separated from the mold release agent).
- An object of the present invention is to provide a water - based mold release agent which is free from the environmental pollution problem during its use, which has excellent dispersibility, storage stability and mold releasability and which gives a good surface state to a molded article of a polymeric material.
- The present invention provides a water-based mold release agent comprising, as a main component, a halogen-containing polyether having at least one functional group.
- The mold release agent according to the present invention comprises
- a) the halogen-containing polyether having at lease one functional group,
- b) a surfactant, and
- c) water.
- The halogen-containing polyether used in the present invention has at least one functional group, and the halogen-containing polyether having no functional group which is described in Japanese Patent Kokai Publication No. 112610/1906 is not preferable in the present invention.
- The halogen-containing polyether having at least one functional group may be well-known one and is described in Japanese Patent Kokai Publication No. 131132/1989 (corresponding to US Patent No. 4,836,944, the disclosure of which is incorporated herein by reference), Japanese Patent Kokai Publication No. 134189/1991, Japanese Patent Kokai Publication No. 268664/1989 (corresponding to US Patent No. 5,004,544, the disclosure of which is incorporated herein by reference), and Japanese Patent Kokai Publication No. 132917/1991.
-
- A perfluoropolyether having a carboxylic acid group or salt thereof is preferable in view of the adherence to a mold surface.
- The halogen-containing polyether preferably has an average molecular weight of 1,000 to 5,000, more preferably 1,500 to 3,500.
- The surfactant used in the present invention may be any of a hydrocarbon surfactant and a fluorine-containing surfactant. Specific examples of the surfactant are Rapizol B-80 (manufactured by Nippon Oil and Fats Co., Ltd.), Nonion NS 230 (manufactured by Nippon Oil and Fats Co., Ltd.), Nonion NS 220 (manufactured by Nippon Oil and Fats Co., Ltd.), Unidine DS 403 (Daikin Industries Ltd.). Among them, the nonionic surfactant is preferable in view of the storage stability. When a nonionic hydrocarbon surfactant is used, the mold release agent is transparent (no cloudiness) and has remarkably excellent storage stability.
- The water-based mold release agent according to the present invention can be prepared, for example, by emulsifying the halogen-containing polyether, the surfactant and water by an ultrasonic homogenizer.
- The water-based mold release agent according to the present invention may further contains d) a phosphate ester or a salt thereof having a pefluoroalkyl group having 4 to 20 carbon atoms. Specific examples of the perfluoroalkyl group-containing phosphate ester are
wherein m is 1 to 9, n is 1, 2 or 3. - In view of the stability, it is preferable that the halogen - containing polyether is emulsified in water and then the perfluoroalkyl group-containing phosphate ester is added to the emulsion.
- The phosphate ester having the perfluoroalkyl group having 4 to 20 carbon atoms gives, for example, excellent releasability for a urethane.
- The water-based mold release agent according to the present invention may contain a silicone or wax compound. The silicone or wax compound improves the surface state of the shaped article so as to reduce a cell collapse, particularly in the case of the polyurethane foam which tends to have the cell collapse.
- Specific examples of the silicone compound are a silicone oil, a silicone resin, a mixture of silicone oil and resin. Specific example of the wax compound is a paraffinic wax.
- The water-based mold release agent according to the present invention comprises
- a) 1 part by weight of the halogen-containing polyether,
- b) 0.02 to 0.8 parts by weight, preferably 0.1 to 0.5 parts by weight of the surfactant, and
- d) 0 to 1.0 parts by weight, preferably 0.1 to 0.8 parts by weight, more preferably 0.2 to 0.3 parts by weight of the perfluoroalkyl group - containing phosphate ester or salt thereof.
- The amount of silicone or wax compound is from 0 to 5.0 parts by weight, preferably from 0 to 1.0 parts by weight per 1 part by weight of the halogen-containing polyether.
- The water-based mold release agent according to the present invention may contain usually 0.1 to 20 % by weight, preferably 0.5 to 10 % by weight of the components other than water c). The mold release agent can be used in a low concentration, migrates to the shaped article in a very low amount, and gives an easy post-treatment (good coating property and adhesion property).
- The mold release agent according to the present invention can be used as an internal mold release agent, but it is preferably used as an external mold release agent. When the mold release agent according to the present invention is coated on a mold, any of a brush coating method, a dip coating method, a spray coating method and the like can be used.
- The mold release agent according to the present invention is useful for the preparation of the shaped article made of a synthetic resin and a rubber, particularly a polyurethane or a polyurea.
- The present invention will be illustrated by the following Examples and Comparative Examples.
- A mold release agent was prepared by emulsifying the components shown in Table 1 at 25°C for 6 minutes by the use of an ultrasonic homogenizer (manufactured by Choonpakogyo Co. Ltd., Output: 300 W).
- Then, the mold release agent was coated on a mold, and a urethane foam was molded from a liquid A and a liquid B shown in Table 2.
- The mold releasability and the surface state of the shaped article were evaluated. A mold release stress (g/cm²) was measured by the use of an autographic device (manufactured by Shimadzu Corp., DCM-50M). The results are shown in Table 3. Table 3 also show stability of the mold release agent.
Table 2 Liquid A Sannix FA-912 Polyol 100 pbw manufactured by Sanyo Chemical Industries Ltd. Ethylene glycol Cross-linking agent 9 pbw (ditto) Flon 11U Foaming agent 15 pbw (ditto) DABCO 33LV Catalyst 4 pbw (ditto) Liquid B Colonate 1040 Isocyanate 65 pbw manufactured by Nippon Polyurethane Ltd. Molding conditions: Mold material aluminum Mold size 5.5 cm diameter x 1.0 cm Stirring time 5,000 rpm x 10 seconds Foaming and curing time 10 minutes Mold temperature 40°C Method of coating the mold release agent brush-coating at room temperature Table 3 Example No. Stability Mold releasability (g/cm²) Surface state 1 Good 160 Good 2 Good 170 Good 3 Good 95 Good 4 Very good 110 Good 5 Very good 125 Good 6 Very good 150 Good 7 Good 150 Good 8 Good 230 Good 9 Good 100 Good 10 Good 150 Good 11 Good 160 Good Com. 1 Bad 190 Good Com. 2 Very good 230 Pinholes formed Com. 3 Very good 300 Good Com. 4 Very good 350 Good Note)
Stability:
Very Good: Transparent (not separated after two weeks)
Good: Milky white (separated after one week)
Bad: Milky white (separated after two days)
Surface state:
Good: No cell collapse - The water-based mold release agent according to the present invention gives no environmental pollution, has excellent dispersibility, storage stability and mold releasability and gives a good surface state to the shaped article of the polymeric material.
- In addition, the water-based mold release agent according to the present invention forms a reversed micelle having the functional group present in water. The water-based mold release agent according to the present invention is adsorbed easily and selectively by the mold surface and can form a tough coating film having good durability. The water-based mold release agent according to the present invention can give more uniform thickness of a coating film than an organic solvent - based mold release agent.
Claims (6)
- A water-based mold release agent comprising, as a main component, a halogen-containing polyether having at least one functional group.
- The water-based mold release agent according to claim 1, which comprisesa) the halogen-containing polyether having at lease one functional group,b) a surfactant, andc) water.
- The water-based mold release agent according to claim 1 or 2, wherein the halogen-containing polyether is a perfluoropolyether.
- The water-based mold release agent according to claim 2 or 3, which further contains d) a phosphate ester or salt thereof having a perfluoroalkyl group having 4 to 20 carbon atoms.
- The water-based mold release agent according to anyone of claims 2 to 4, wherein the surfactant is a nonionic surfactant.
- The water-based mold release agent according to anyone of claims 1 to 5, wherein the functional group is a carboxylic acid group or salt thereof.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4109566A JPH05301228A (en) | 1992-04-28 | 1992-04-28 | Release agent |
JP10956692 | 1992-04-28 | ||
JP109566/92 | 1992-04-28 | ||
PCT/JP1993/000544 WO1993022121A1 (en) | 1992-04-28 | 1993-04-27 | Parting agent |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0597115A4 EP0597115A4 (en) | 1994-03-08 |
EP0597115A1 true EP0597115A1 (en) | 1994-05-18 |
EP0597115B1 EP0597115B1 (en) | 2001-08-22 |
Family
ID=14513496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93909426A Expired - Lifetime EP0597115B1 (en) | 1992-04-28 | 1993-04-27 | Parting agent |
Country Status (7)
Country | Link |
---|---|
US (1) | US5525150A (en) |
EP (1) | EP0597115B1 (en) |
JP (1) | JPH05301228A (en) |
KR (1) | KR100281221B1 (en) |
DE (1) | DE69330631T2 (en) |
SG (1) | SG54124A1 (en) |
WO (1) | WO1993022121A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995017288A1 (en) * | 1993-12-22 | 1995-06-29 | Bayer Aktiengesellschaft | Process for producing composites |
EP0759348A1 (en) * | 1994-05-11 | 1997-02-26 | Daikin Industries, Limited | Molding method and diluent for mold release agent |
WO2001017743A1 (en) * | 1999-09-02 | 2001-03-15 | Nanogate Gmbh | Reactive release agent for stripping synthetic resins |
WO2003045656A1 (en) * | 2001-11-28 | 2003-06-05 | Bayer Materialscience Ag | Mould release agents and method for the production of plastic moulding parts |
WO2010046464A1 (en) * | 2008-10-24 | 2010-04-29 | Solvay Solexis S.P.A. | Method for forming a lubricating film |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5746961A (en) * | 1995-12-04 | 1998-05-05 | Michael J. Stevenson | Method for enhancement of the surfaces of molded plastic products |
JP4524943B2 (en) * | 2001-03-27 | 2010-08-18 | ダイキン工業株式会社 | Method for forming pattern of semiconductor element and method for manufacturing mold for imprint processing |
WO2003085023A1 (en) * | 2002-04-10 | 2003-10-16 | Sanyo Chemical Industries, Ltd. | Polyurethane resin based slush molding material |
US20060108710A1 (en) * | 2004-11-24 | 2006-05-25 | Molecular Imprints, Inc. | Method to reduce adhesion between a conformable region and a mold |
US20060032600A1 (en) * | 2004-08-10 | 2006-02-16 | Signicast Corporation | Mold releasable pattern material for use in investment casting |
WO2006057843A2 (en) | 2004-11-24 | 2006-06-01 | Molecular Imprints, Inc. | Method and composition providing desirable characteristics between a mold and a polymerizable composition |
US7674928B2 (en) * | 2006-11-13 | 2010-03-09 | E.I. Du Pont De Nemours And Company | Polyfluoroether-based phosphates |
US20090041986A1 (en) * | 2007-06-21 | 2009-02-12 | 3M Innovative Properties Company | Method of making hierarchical articles |
US20080315459A1 (en) * | 2007-06-21 | 2008-12-25 | 3M Innovative Properties Company | Articles and methods for replication of microstructures and nanofeatures |
US20090114618A1 (en) * | 2007-06-21 | 2009-05-07 | 3M Innovative Properties Company | Method of making hierarchical articles |
US20100109195A1 (en) | 2008-11-05 | 2010-05-06 | Molecular Imprints, Inc. | Release agent partition control in imprint lithography |
JP5621775B2 (en) * | 2009-09-08 | 2014-11-12 | ダイキン工業株式会社 | New nonionic surfactant and anti-fogging agent |
JP4626715B1 (en) * | 2009-09-11 | 2011-02-09 | ユニマテック株式会社 | Release agent |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59166596A (en) * | 1983-03-14 | 1984-09-19 | Nippon Mektron Ltd | Mold release agent |
EP0310966A1 (en) * | 1987-10-02 | 1989-04-12 | AUSIMONT S.p.A. | Additives coadjuvating the detaching from the molds of rubbers vulcanizable by means of peroxides |
EP0315078A2 (en) * | 1987-10-28 | 1989-05-10 | AUSIMONT S.p.A. | Aqueous microemulsions comprising functional perfluoropolyethers |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58180598A (en) * | 1982-04-19 | 1983-10-22 | Nippon Mektron Ltd | Mold releasing agent |
JPS5932513B2 (en) * | 1982-05-14 | 1984-08-09 | ダイキン工業株式会社 | Release agent |
JPS5932513A (en) * | 1982-08-13 | 1984-02-22 | Nissan Motor Co Ltd | Air-conditioner duct |
JPS61112610A (en) * | 1984-11-07 | 1986-05-30 | Daikin Ind Ltd | Release agent |
JP2658172B2 (en) * | 1988-05-11 | 1997-09-30 | ダイキン工業株式会社 | Release agent |
JP2658179B2 (en) * | 1988-05-19 | 1997-09-30 | ダイキン工業株式会社 | Release agent |
-
1992
- 1992-04-28 JP JP4109566A patent/JPH05301228A/en active Pending
-
1993
- 1993-04-27 US US08/170,210 patent/US5525150A/en not_active Expired - Lifetime
- 1993-04-27 WO PCT/JP1993/000544 patent/WO1993022121A1/en active IP Right Grant
- 1993-04-27 EP EP93909426A patent/EP0597115B1/en not_active Expired - Lifetime
- 1993-04-27 KR KR1019930704053A patent/KR100281221B1/en not_active IP Right Cessation
- 1993-04-27 DE DE69330631T patent/DE69330631T2/en not_active Expired - Fee Related
- 1993-04-27 SG SG1996001270A patent/SG54124A1/en unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59166596A (en) * | 1983-03-14 | 1984-09-19 | Nippon Mektron Ltd | Mold release agent |
EP0310966A1 (en) * | 1987-10-02 | 1989-04-12 | AUSIMONT S.p.A. | Additives coadjuvating the detaching from the molds of rubbers vulcanizable by means of peroxides |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1995017288A1 (en) * | 1993-12-22 | 1995-06-29 | Bayer Aktiengesellschaft | Process for producing composites |
EP0759348A1 (en) * | 1994-05-11 | 1997-02-26 | Daikin Industries, Limited | Molding method and diluent for mold release agent |
US5853646A (en) * | 1994-05-11 | 1998-12-29 | Daikin Industries, Ltd. | Molding method and dilution agent for mold releasing agent |
EP0759348B1 (en) * | 1994-05-11 | 2003-07-23 | Daikin Industries, Limited | Molding method and diluent for mold release agent |
WO2001017743A1 (en) * | 1999-09-02 | 2001-03-15 | Nanogate Gmbh | Reactive release agent for stripping synthetic resins |
WO2003045656A1 (en) * | 2001-11-28 | 2003-06-05 | Bayer Materialscience Ag | Mould release agents and method for the production of plastic moulding parts |
US6841115B2 (en) | 2001-11-28 | 2005-01-11 | Bayer Aktiengesellschaft | Mold release agent and process for the production of plastic molded parts |
CN1596178B (en) * | 2001-11-28 | 2011-03-16 | 拜尔材料科学股份公司 | Mold release agent and method for producing plastic molded parts |
WO2010046464A1 (en) * | 2008-10-24 | 2010-04-29 | Solvay Solexis S.P.A. | Method for forming a lubricating film |
CN102197118A (en) * | 2008-10-24 | 2011-09-21 | 索尔维索莱克西斯公司 | Method for forming a lubricating film |
US9005711B2 (en) | 2008-10-24 | 2015-04-14 | Solvay Specialty Polymers Italy S.P.A. | Method for forming a lubricating film |
Also Published As
Publication number | Publication date |
---|---|
JPH05301228A (en) | 1993-11-16 |
SG54124A1 (en) | 1998-11-16 |
EP0597115B1 (en) | 2001-08-22 |
US5525150A (en) | 1996-06-11 |
DE69330631T2 (en) | 2002-07-04 |
DE69330631D1 (en) | 2001-09-27 |
EP0597115A4 (en) | 1994-03-08 |
KR940701327A (en) | 1994-05-28 |
WO1993022121A1 (en) | 1993-11-11 |
KR100281221B1 (en) | 2001-04-02 |
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